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Corneal dystrophy, Fuchs endothelial, 8

MONDO:0014228

Any Fuchs' endothelial dystrophy in which the cause of the disease is a mutation in the AGBL1 gene.

Also known as: AGBL1 Fuchs' endothelial dystrophy, Fuchs' endothelial dystrophy caused by mutation in AGBL1, corneal dystrophy, Fuchs endothelial, 8, corneal dystrophy, Fuchs endothelial, type 8, FECD8

16 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Hereditary disease (172) Eye disorder (97) Corneal disorder (39) Fuchs' endothelial dystrophy (27) Human disease (14) Corneal dystrophy (4) Corneal endothelial dystrophy (3) Disorder of orbital region (3) Disease of genetic or genomic mechanism (2)

Trials to join now! 11 Not yet recruiting 1 Not yet finished but already full! 1 Completed 2 Terminated 1

VR headsets tested as a possible treatment for blindness

Disease control Terminated

This study tested whether using a virtual reality headset for one-hour sessions could help regenerate damaged optic nerves and improve vision in people with glaucoma or other retinal diseases. The idea came from promising results in rodents. However, the trial was terminated earl…

Phase: NA • Sponsor: Stanford University • Aim: Disease control

Last updated Jun 27, 2026 08:03 UTC